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1-Chloro-4-Iodobenzene

    • Product Name 1-Chloro-4-Iodobenzene
    • Alias p-Chloroiodobenzene
    • Einecs 214-989-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    893189

    Chemical Name 1-Chloro-4-Iodobenzene
    Molecular Formula C6H4ClI
    Molar Mass 238.45 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 66-70 °C
    Boiling Point 265-267 °C
    Density 2.04 g/cm³
    Cas Number 637-87-6
    Smiles ClC1=CC=C(C=C1)I
    Pubchem Cid 12212
    Refractive Index 1.65
    Solubility In Water Insoluble

    As an accredited 1-Chloro-4-Iodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with screw cap, 25g label: "1-Chloro-4-Iodobenzene, C6H4ClI, CAS 637-87-6, Keep tightly closed, for laboratory use."
    Shipping 1-Chloro-4-iodobenzene is shipped in tightly sealed containers, typically made of glass or suitable inert materials, under cool, dry conditions. Proper labeling for hazardous materials is required, and transport complies with relevant regulations for halogenated aromatic compounds. Avoid exposure to heat, moisture, and direct sunlight during shipping.
    Storage 1-Chloro-4-iodobenzene should be stored in a tightly sealed container, away from incompatible substances such as strong oxidizing agents. Keep in a cool, dry, well-ventilated area, protected from direct sunlight and sources of heat or ignition. Store at room temperature, and clearly label the container. Ensure access is limited to trained personnel and incorporate appropriate spill containment measures.
    Application of 1-Chloro-4-Iodobenzene

    Applications of 1-Chloro-4-Iodobenzene in Industrial Manufacturing

    As an experienced chemical raw material manufacturer, we supply 1-Chloro-4-Iodobenzene for multiple advanced industrial value chains. The following sections highlight its integration into key production processes, including the required industry standards, dosage recommendations, process implementation, and the principal types of end use products.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    1-Chloro-4-Iodobenzene acts as an essential halogenated building block for the synthesis of complex pharmaceutical molecules, particularly in the creation of biaryl structures and substituted anilines. API manufacturers leverage its dual halogen functionalities to enable specific cross-coupling reactions during the intermediate stages of drug synthesis. This material is critical for molecular scaffolding in anti-cancer agents, anti-infectives, and certain CNS pharmaceuticals. Diphenylamine derivatives and benzamide frameworks commonly originate from this compound within regulated pharmaceutical manufacturing environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters <825> and <1072> for materials handling
    • 21 CFR Part 210/211 (US FDA cGMP for drugs)
    • Directive 2001/83/EC (EU Medicines for Human Use)

    Typical usage ratio

    • 0.5–2.5 molar equivalents per target scaffolding reaction, adjusted according to coupling efficiency and purification step requirements

    Downstream process integration

    • Feeds into the Suzuki-Miyaura or Buchwald–Hartwig cross-coupling stage, preceding hydrolysis and final purification of intermediates

    Final product types

    • API intermediates for oncology, CNS, antiviral, or cardiovascular drugs
    • Biphenyl carboxamides used in finished medicines after downstream elaboration

    2. Agrochemical Intermediate for Herbicide & Fungicide Synthesis

    The compound serves as a versatile molecular precursor in the production of advanced agrochemicals, primarily certain broad-spectrum herbicides and fungicides based on biaryl or heteroaryl motifs. Specialty fine chemical plants utilize its halogen functions for palladium-catalyzed coupling or Ullmann-type processes, generating key intermediates that coordinate with other functional groups for improved activity and environmental profile. Use in large-scale synthesis is strictly regulated to maintain batch-to-batch reproducibility and residual impurity thresholds.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (AGP:CPP)
    • ISO 9001:2015 (Quality Management for chemical production)
    • REACH Regulation (EC) No 1907/2006 for chemical safety in the EU
    • China GB /T 37959 – National pesticide intermediate safety standard

    Typical usage ratio

    • 0.8–1.2 molar ratios based on stoichiometry of coupling steps; varies by downstream product class and targeted impurity profile

    Downstream process integration

    • Introduced at aryl halide activation phase for C–C and C–N bond formation in batch or continuous line synthesis, before oxidation or isomerization steps

    Final product types

    • Biphenyl-based selective herbicides
    • Fungicidal intermediates later formulating into market-ready crop protection agents

    3. Performance Material Intermediate in Liquid Crystal Manufacturing

    In liquid crystal manufacturing for display and specialty electronics, 1-Chloro-4-Iodobenzene contributes to the synthesis of mesogenic compounds with tailored polarity and dielectric properties. The compound’s halogen layout permits selective functionalization yielding a series of high-purity, structurally precise biphenyl derivatives. These downstream molecules are essential in defining phase transition temperatures, optical anisotropy, and electro-optical properties within advanced LCD and OLED devices.

    Industry compliance standards

    • IPC-4101 specification for base materials for printed boards
    • RoHS Directive 2011/65/EU regarding hazardous substances in electronics
    • JIS C6109 (Japan Industrial Standards for liquid crystal media)
    • IEC 61249-2 for materials and process control

    Typical usage ratio

    • 1.0–1.5 molar equivalent per finalized biphenyl or terphenyl unit, depending on target mesogen chain length and purity demands

    Downstream process integration

    • Introduced at aryl coupling and halogen exchange stage during fine synthesis of mesogenic intermediates, often under anhydrous and inert conditions

    Final product types

    • Biphenyl-based and terphenyl-based liquid crystal compounds used in TFT-LCD and advanced display panels
    • Specialty mixtures for OLED backplane materials

    4. Advanced Material Precursor in Organic Synthesis for Specialty Polymers

    Chemical processors employ 1-Chloro-4-Iodobenzene as an initial functionalized aromatic in polymer R&D and niche high-performance polymer production. It enables the stepwise construction of fluoro-, amino-, or additional halogen-substituted monomers. These specialized monomers impart targeted solubility, thermal stability, or flame retardance to downstream specialty polyimide fibers, electronic encapsulation compounds, or advanced engineering plastics. The integration focuses on high conversion rates and contaminant minimization for electronics and aerospace regulatory requirements.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 (Quality and Environmental Management)
    • UL 94 (flammability for polymer materials)
    • ASTM D4066 (Classification for Nylon and Polyamide Molding and Extrusion)
    • IPC-4101 (base materials for printed circuit polymers)

    Typical usage ratio

    • Varies from 0.2 up to 2.0 molar ratios per monomer synthesis batch, according to engineered polymer backbone and desired end-group transformation

    Downstream process integration

    • Integrated during aromatic monomer synthesis via halide exchange, amidation, or direct arylation before polymerization to final resin

    Final product types

    • Specialty polyimides for flexible electronics
    • High-temperature resins used in chip packaging and aerospace composite materials

    5. Fine Chemical Intermediate for Dyes & Pigments Manufacturing

    The aryl halide is a reliable intermediate for synthesizing several high-performance industrial dyes and pigments, where selective substitution on the benzene ring is required. Its controlled reactivity supports the formation of azo, anthraquinone, and diaryl pigment precursors, contributing to color formulation for application in technical fibers and high-durability coatings. Integration into pigment synthesis emphasizes color strength, fastness, and environmental compliance, with strict controls over aromatic substitution efficiency.

    Industry compliance standards

    • EN 71-3:2019 (chemical safety for colorants in toys and textiles)
    • REACH Annex XVII (restrictions on use of azo dyes in Europe)
    • OEKO-TEX Standard 100 (textile and dye safety)
    • ISO 105-X12 (Color fastness to rubbing for textiles)

    Typical usage ratio

    • 0.5–1.8 molar equivalents relative to target chromophore, depending on substitution site and dye class requirements

    Downstream process integration

    • Added during initial aromatic halogenation or coupling in pigment intermediate synthesis, preceding azo condensation or cyclization stages

    Final product types

    • High-purity azo and anthraquinone dyes for synthetic fibers
    • Disperse and pigment-grade colorants used in industrial coatings, plastics, and inks
    Free Quote

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    Certification & Compliance
    More Introduction

    1-Chloro-4-Iodobenzene: Where Precision Chemistry Meets Real-World Need

    A Direct View From the Factory Floor

    Anyone who works with fine chemicals sees how finished molecules build up from the simplest reactions. In our workshops, every flask that leaves the shelf carries the mark of someone who has measured, checked, and confirmed the details of every batch. 1-Chloro-4-iodobenzene is among those products that keep us on our toes. This compound looks tame in a bottle: a clear, pale crystalline powder, usually stored in brown glass jars to avoid any trace of light-driven decomposition. But behind the simple appearance is a versatile intermediate that plays a role for both the researcher pushing the boundaries of organic synthesis and the production chemist looking to expand a library of halogenated aromatics.

    Crafting 1-Chloro-4-Iodobenzene: Not Just About Making Molecules

    Our story with this molecule begins with careful selection of starting materials. Benzene derivatives can’t all be handled the same way—stability, cost, and purity of feedstocks really matter. To make 1-chloro-4-iodobenzene efficiently and safely, we rely on our long-developed process controls, not just recipe following. Each batch starts by chlorinating the benzene ring under tightly monitored reaction conditions; without close monitoring, side products and isomeric impurities sneak in, complicating downstream use. The next stage, the introduction of iodine, requires even more diligence. Iodination doesn’t only depend on stoichiometry but on reaction temperature, solvent control, and—above all—scrupulous purification.

    There’s often a temptation in this business to use the cheapest sources and fastest methods available, but those who have worked up a pound of this compound know what it means to have recurrent issues with palladium contamination, hydrochloric acid residues, or unwanted dihalogenated byproducts. We understand the invisible costs of these shortcuts: glassware that degrades, laboratory scales that dance out of calibration from sticky residue, frustrated R&D teams troubleshooting failed cross-coupling reactions. Investment in reliable purification technologies pays off in the results we can confidently ship out, and our experience has shown time and again that trace contaminants can hold back an entire downstream process.

    Specifications: Beyond the Purity Number

    Most technical datasheets quote broad figures—purity above 98%, melting points between 62–65°C, storage below 25°C, and so on. Years of hands-on production remind us that such figures only make sense with a human eye on every batch. Recrystallization techniques and analytical systems (GC, HPLC, NMR, IR) aren’t just about hitting number targets but about matching how those numbers fit in process conditions. It’s not just purity on paper but functional purity in a real reaction environment, free from scavengers, inhibitors, or color bodies that interfere with catalysis or extraction downstream.

    We focus particularly on minimizing residual solvents and making sure halogen content is balanced. Too much free chlorine from over-chlorination, for instance, can trigger corrosion in customer glassware or cause unwanted polymerization during scale-up. On the other hand, poorly purified batch with chloride or iodide ions can easily cause erratic results in Suzuki reactions, which is where this molecule comes into its own.

    Use Cases: Real-World Applications in Chemistry

    1-Chloro-4-iodobenzene matters in synthesis because it serves both as a reliable electrophile in coupling reactions and as a dual-source halogen for further functionalization. Researchers see most value in its use for Suzuki, Stille, or Sonogashira cross-couplings. Because it contains both a chlorine and an iodine atom on opposite sides of the aromatic ring, chemists can selectively substitute at one site or the other, opening the door for combinatorial library formation or the synthesis of advanced materials.

    In our experience, the iodine handle often gets targeted first. Palladium-catalyzed couplings grab the iodo-position thanks to its superior leaving group ability, leaving the chlorine behind for future steps. This approach lets medicinal chemists walk across a molecule, stepwise, adding complexity as they go—friendly to both scale-up for patent work and discovery-stage screening. Those in the field of materials science, electronics, or photoactive systems use this compound as a key intermediary to stitch together larger aromatic systems, as seen in the assembly of OLED (organic light-emitting diode) precursors, advanced polymers, and sensors.

    Value also shows up for those in the agricultural and environmental chemistry space. Halogenated aromatics feature in many agrochemicals and specialty reagents. Because 1-chloro-4-iodobenzene allows for tight control over substitution, it easily integrates into multi-step synthesis routes for pesticides and herbicide candidates or for the preparation of analytical standards.

    Comparing Real Differences With Other Halobenzenes

    It sounds simple: a benzene ring with two halogens. But veterans of aryl halide work see quickly that placement and type of halogen make or break a synthetic plan. 1,4-Dichlorobenzene and 1,4-diiodobenzene, for example, can’t substitute for 1-chloro-4-iodobenzene in selective chemistry. The big difference lies in reactivity and site-selectivity. The iodo group in our molecule leaves much more readily than the chloro. Dual-halogenated aromatics with only chlorine or only iodine lack this stepwise control—react too fast, or not at all, under common catalysis.

    This difference becomes practical in a kilo-lab setting where chemists want to build unsymmetrical products. For instance, the process of making biphenyl systems with distinct substituents often uses our compound rather than simpler halogen combinations. By letting the more reactive iodine leave during the first coupling, the remaining chloro position serves as a handle for a later, more robust transformation. The final sequence runs smoother and produces higher yields without fighting unreacted starting material or byproducts—a lesson many process developers have learned the hard way.

    Challenges in Continuous Supply and Quality Control

    A factory is only as good as its consistency. For compounds like 1-chloro-4-iodobenzene, market needs swing widely based on changes in pharmaceutical R&D budgets, changes in patent landscapes, or new material developments. Sudden spikes put stress on everything from raw material inventories to QA/QC systems.

    From years on this line, we’ve seen that sudden demand puts stress on procurement of high-purity iodo and chloro reagents, which aren’t always available at scale. Iodine pricing in particular behaves erratically, sometimes swinging as much as 50% in a calendar quarter. We keep a rolling stock of key raw materials and keep vendor relationships open so as to guarantee continuity of supply, even during global disruptions.

    Another headache comes from balancing short-run, highly customized orders against long-run bulk batches. Smaller R&D units want a few hundred grams of ultra-pure, freshly prepared product. Downstream manufacturing calls for drum quantities with guaranteed batch-to-batch traceability, which demands robust documentation and a systematic approach to cleaning and changeovers. We learned long ago to schedule smaller, bespoke runs early in production cycles and reserve full-day lines for larger campaigns, always with gaps for cleaning and verification. This approach helps prevent cross-contamination and assures everyone—especially those working with trace catalysts or in high-value synthesis—gets material that fits their needs.

    Environmental and Safety Considerations In Practice

    Handling dual-halogenated aromatics like 1-chloro-4-iodobenzene calls for a precise respect for health, safety, and the environment. Both the iodine reagents and the finished product pose particular risks, from skin and eye exposure to more severe chronic hazards related to inhalation or environmental release.

    On the shop floor, staff never rely just on fume hoods. We maintain rigorous air filtration and spill remediation procedures. Waste handling requires the export of spent halogenated solvents and residuals to certified destruction facilities. Each batch process is engineered to minimize excess reactivity, avoid runaway exotherms, and keep operator exposure safely below published limits. We update our training for every new regulation and regularly run drills on containment and response—for safety, experience proves more important than the best-written procedure.

    Environmental compliance isn’t just a box to check; it’s a part of our plant culture. Water used in washing and processing never goes straight to drain but passes through multi-stage capture and treatment. Onsite air scrubbers neutralize volatile iodides, and we keep a persistent log of actual emissions, not just theoretical figures. After years in this trade, staying ahead of regulations makes good sense—it’s always less costly to prevent a problem than to pay for one.

    Meeting Evolving Demands Through Experience

    Chemistry keeps moving. Regulatory pressures—think REACH, GHS, and new standards in occupational exposure—change how manufacturers need to operate. We have shifted processes over the last decade, adapting batch recordkeeping to digital ERP systems and integrating advanced analytical monitoring at each step. The push for green chemistry has spurred us to examine how we handle waste and search for milder reaction conditions or better atom economies.

    We also recognize that the demands of modern research call for flexibility. Some customers need lot-specific COAs (Certificates of Analysis) with detailed impurity profiles, others prioritize eco-friendly labeling, and still others ask for support troubleshooting reactions using our material. Long hours troubleshooting a stubborn palladium-catalyzed bond formation have given us a taste for how details in raw material trace contaminants show up as persistent reaction problems. We keep open lines with clients from academia to industry, providing feedback and hearing about real successes or failures from their own efforts.

    Technical Support Rooted in Real Experience

    Having our own production lines means we track down cause-and-effect instead of giving broad advice. Run into a strange color or persistent impurity in a batch? We’ve likely seen it, traced it, and worked out a way around it. Our support for process chemists extends beyond simply shipping containers down the loading dock. If questions arise about reaction mechanics or best conditions—solvent choices, base compatibility, phosphine ligand selection, or even the sequence of adding reagents—we can pull from actual production logs, not just literature searches.

    We’ve walked clients through solvent exchanges to improve coupling yields, advised on storage of finished products to limit decomposition (always cool, dry, and dark), and even stepped in to troubleshoot glassware corrosion or unexplained yield drops. In every case, our experience proves that small details add up to big impacts in halogenated aromatic chemistry.

    What Sets Our Product Apart: Quality Built on Track Record

    Years of trial and error have taught us that buyers often pay more in lost time than in price per kilo. For customers needing reliable, repeatable results, 1-chloro-4-iodobenzene made by hand (and eye) from a trustworthy team proves its value in less batch-to-batch troubleshooting, fewer regulatory headaches, and real cost-control over multi-stage synthetic plans.

    What we send out isn’t just a chemical. It reflects the learning and sweat of those behind every kilogram—from chemists mixing reaction vessels at 4 am to QA managers reviewing impurity maps. Our approach leads to fewer recalls, fewer out-of-spec rejections, and happier process chemists all the way through the supply chain. We’ve seen customers build entire new product lines on the strength of our intermediate; their wins drive us to keep investing in know-how, technology, and people.

    Pushing Chemistry Forward—Responsibly

    The market for 1-chloro-4-iodobenzene will never be as large or as high-profile as some big-volume industrial chemicals. But for those who depend on it, quality matters far more than quantity. We believe that modern chemical manufacturing doesn’t just play defense—complying with new laws, avoiding mistakes, or chasing after problems—but should take the lead in anticipating client needs, making processes safer, and contributing to a more sustainable future.

    That means linking every barrel or drum not to a faceless process but to people who care deeply about their craft. By applying all our learning, investing in smart plant design, and training up new craftsmen and women, we make sure that every container doesn’t just meet a spec, but gives a head start to everyone who puts the material to use in the lab or on the line.

    Our story with 1-chloro-4-iodobenzene doesn’t end at the shipping dock. Each batch shapes the research of partners in pharmaceuticals, materials science, and green chemistry. With every improvement in process or purity, we keep pushing chemistry forward, one reaction at a time.